Dazomet

Source: Wikipedia, the free encyclopedia.
Dazomet
Names
Preferred IUPAC name
3,5-Dimethyl-1,3,5-thiadiazinane-2-thione
Other names
Mylon; Basamid, Thiazone; Mylone; Tiazon; DMTT; Dimethylformocarbothialdine; Carbothialdin; Basamide; Nefusan; Prezervit
Identifiers
3D model (
JSmol
)
ChemSpider
ECHA InfoCard
 100.007.798 Edit this at Wikidata
UNII
  • InChI=1S/C5H10N2S2/c1-6-3-7(2)5(8)9-4-6/h3-4H2,1-2H3
    Key: QAYICIQNSGETAS-UHFFFAOYSA-N
  • CN1CN(C(=S)SC1)C
Properties
C5H10N2S2
Molar mass 162.27 g·mol−1
Appearance White solid
Density 1.29±0.1 g/mL[1]
Melting point 104 to 105 °C (219 to 221 °F; 377 to 378 K)
Boiling point 222.3±50.0 °C (predicted)[1]
Hazards
Flash point 156 °C (313 °F)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Dazomet is a common soil

fumigant that acts as a herbicide, fungicide, slimicide,[3] and nematicide
.

Applications

Dazomet is a chemical used to kill pests that inhibit plant growth through gaseous degradation. Dazomet is used as a soil sterilant on a variety of sites such as golf courses, nurseries, turf sites, and potting soils.

Phellinus noxius, or brown root rot disease.[5]

Synthesis

Dazomet is synthesized from carbon disulfide (CS2) and diluted methylamine (CH3NH2). After stirring for 1-2 hours, an oily substance is formed, which is the intermediate methyldithiocarbamic acid (HS2CNHCH3). Then, formaldehyde (CH2O) is added to the intermediate to form and precipitate out the dazomet.[6]

Form, color, and smell

Dazomet takes the form of colorless crystals.[7][8] Dazomet is described as having a weakly pungent[9] smell.

Toxicology and safety

Dazomet is irritating to the eyes[10] and its degradation product, MITC, is a dermal sensitizer. Dazomet is very toxic to aquatic organisms, and also acutely toxic to mammals. Exposure to dazomet can occur through several means; interaction with unincorporated granules, inhalation of it decomposition product, MITC, and/or water runoff.

Stability and shelf life

Dazomet is stable at temperatures up to 35°C; it is sensitive to temperature >50°C and to moisture.[7][11] Dazomet has a shelf life of at least two years when stored below 50°C.[12]

Mass spectrum

The molecular ion peak of dazomet is at 162 m/z. There are two major fragment peaks, one at 89 m/z and one at 42 m/z. The fragment peak at 89 m/z represents the loss of MITC, which is the major, gaseous degrade of dazomet.[13]

Patents

Patent #US5989597
Ambrose Rajamannan was the inventor of the novel process of continuously and instantaneously sterilizing soil using a water-activated fumigant. Dazomet is one water-activated fumigant that could be used. This process ensures 100% activation of the fumigant. Therefore, less fumigant would be needed to ensure that the soil would be completely sterilized.[14]
Patent #CN1543787
See under § Synthesis

References

  1. ^ a b SciFinder.Dazomet.properties (accessed Oct. 5, 2014).
  2. ^ "MSDS for Diazomet". Sigma-Aldrich.
  3. ^ "Revised Environmental ate and Ecological Risk Assessment for Dazomet" (https://www3.epa.gov/pesticides/chem_search/cleared_reviews/csr_PC-035602_08-Apr-08_a.pdf) (PDF) US Environmental Protection Agency, Office of Prevention, Pesticides, and Toxic Substances. April 8, 2008.
  4. US Environmental Protection Agency, Office of Pesticide Programs. July 10, 2008. Archived from the original (PDF) on 2014-10-16. {{cite journal}}: Cite journal requires |journal= (help
    )
  5. ^ Fu, C.; Hu, B.; Chang, T.; Hsueh, K.; Hsu, W. Evaluation of dazomet as fumigant for the control of brown root rot disease. Pest Management Science 2012, 68, 959-962.
  6. ^ Cao, Y.; Lu, Y. Process for preparing dazomet dustless stable fine granules. CN1543787, Nov. 10, 2004.
  7. ^ a b "Dazomet". PubChem. National Center for Biotechnology Information. Retrieved 2021-11-12.
  8. ^ Tomlin CDS, ed; The e-Pesticide Manual: a world compendium. Dazomet. 13th ed. PC CD-ROM, Version 3.0, 2003-04. Surrey, UK: British Crop Protection Council, (2003)
  9. ^ Meister, R.T., Sine, C. (eds) Crop Protection Handbook Volume 92, Willoughby, OH, 2006., p. D 127
  10. ECHA
    . Retrieved 2019-02-11.
  11. ^ Tomlin, C.D.S. (ed.). The Pesticide Manual - World Compendium. 10th ed. Surrey, UK: The British Crop Protection Council, 1994., p. 280
  12. ^ Hartley, D. and H. Kidd (eds.). The Agrochemicals Handbook. Old Woking, Surrey, United Kingdom: Royal Society of Chemistry/Unwin Brothers Ltd., 1983., p. A114/Oct 83
  13. ^ NIST Chemistry WebBook. 2H-1,3,5-Thiadiazine-2-thione, tetrahydro-3,5-dimethyl-. http://webbook.nist.gov/ (accessed Oct. 5, 2014).
  14. ^ Rajamannan, A. H. J. Process for sterilizing soil. US Patent 5989597, Nov. 23, 1999.
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